A) Promoting Justice
B) Promoting Health and Well-Being
C) Maintaining Privacy and Confidentiality
D) Promoting and Respecting Informed Decision Making
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verified
Multiple Choice
A) Promoting Justice
B) Promoting Health and Well-Being
C) Maintaining Privacy and Confidentiality
D) Preserving Dignity
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verified
Multiple Choice
A) approval of the research design.
B) protecting participants from undue risk.
C) ensuring that informed consent is obtained.
D) promotion of nursing research in health care institutions.
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verified
Multiple Choice
A) Intent to harm
B) Fraudulent behaviour
C) Scientific misconduct
D) Unauthorized research
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verified
Multiple Choice
A) Right to fair treatment
B) Right to self-determination
C) Right to privacy and confidentiality
D) Right to anonymity
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verified
Multiple Choice
A) Justice
B) Beneficence
C) Confidentiality
D) Respect for persons
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verified
Multiple Choice
A) Justice
B) Beneficence
C) Confidentiality
D) Respect for persons
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verified
Multiple Choice
A) A parental signature is required for a child to participate in a study.
B) The study protocol is reviewed with the parent and not the child.
C) The child should be able to express a preference for participation.
D) A child older than age 16 does not require a parent's signature for consent.
E) The child should understand the purpose of the study.
Correct Answer
verified
Multiple Choice
A) Promoting Justice
B) Promoting Health and Well-Being
C) Maintaining Privacy and Confidentiality
D) Preserving Dignity
Correct Answer
verified
Multiple Choice
A) Right to self-determination
B) Right to anonymity and confidentiality
C) Right to fair treatment
D) Right to protection from discomfort and harm
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verified
Multiple Choice
A) It is turned over to the agency's REB for safekeeping.
B) It is sent to the Canadian Institutes of Health Research as evidence of compliance.
C) It is copied; one copy is given to the participant and the other is filed by the researcher in a secured location.
D) There is not special procedure for handling a consent form.
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verified
Multiple Choice
A) Participants may be related to each other.
B) The researcher meets participants face to face in such studies.
C) Participants are not asked to sign an informed consent statement.
D) Verbatim quotations from participants may reveal personal information.
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verified
Multiple Choice
A) Voluntary consent
B) Freedom from harm
C) Protection from discomfort
D) Fair and equitable treatment
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Multiple Choice
A) it is difficult to include both genders.
B) female hormones may interact with the drugs studied.
C) women are generally more difficult to recruit as participants.
D) female participants may not realize they are pregnant, thus putting the fetus at risk.
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Multiple Choice
A) The relevance of the research to issues important to older adults
B) The ethnic background of the potential participant
C) The age of the potential participant
D) The cognitive capacity of the potential participant
E) The degree of risk associated with the study
Correct Answer
verified
Multiple Choice
A) Contact the hospital's REB.
B) Confront the researcher with your concerns.
C) Document your suspicions in the patient's medical record.
D) Secretly record the researcher's interaction with the patient.
Correct Answer
verified
Multiple Choice
A) The witnessing signature of an authorized party
B) The listing of members of the agency's REB
C) Explanation of whom to contact regarding any area of the study
D) List of participant's assignment to intervention group or control group
Correct Answer
verified
Multiple Choice
A) Confront the researcher with concerns.
B) Document suspicions in the patient's medical record.
C) Contact the hospital's REB.
D) Secretly record the researcher's interaction with a potential participant.
Correct Answer
verified
Multiple Choice
A) Respect
B) Beneficence
C) Trust
D) Justice
E) Anonymity
F) Confidentiality
Correct Answer
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Multiple Choice
A) "Patients who were contacted by study personnel and who signed (or whose proxy signed) informed consent were enrolled in the study cohort."
B) "The research has been reviewed and approved by the Human Participants' Review Committee, which include Jane Doe and John Smith."
C) "If you have any concerns about the conduct of this study or your rights as a research participant, please contact Jay Tee, lead investigator for this project atβ¦"
D) "You have been randomly assigned to the intervention group, which will receive a new experimental drug developed to prevent breast cancer."
Correct Answer
verified
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